IRSD, INSERM, INRAE, ENVT, Université de Toulouse, UPS, CHU Purpan, Place du Dr Baylac, CEDEX 3, 31024 Toulouse, France.
Cells. 2021 Jan 24;10(2):225. doi: 10.3390/cells10020225.
In adult stem cells, Glycogen Synthase Kinase 3β (GSK3β) is at the crossroad of signaling pathways controlling survival, proliferation, adhesion and differentiation. The microenvironment plays a key role in the regulation of these cell functions and we have demonstrated that the GSK3β activity is strongly dependent on the engagement of integrins and protease-activated receptors (PARs). Downstream of the integrin αβ or PAR activation, a molecular complex is organized around the scaffolding proteins RACK1 and β-arrestin-2 respectively, containing the phosphatase PP2A responsible for GSK3β activation. As a consequence, a quiescent stem cell phenotype is established with high capacities to face apoptotic and metabolic stresses. A protective role of GSK3β has been found for hematopoietic and intestinal stem cells. Latters survived to de-adhesion through PAR activation, whereas formers were protected from cytotoxicity through αβ engagement. However, a prolonged activation of GSK3β promoted a defect in epithelial regeneration and a resistance to chemotherapy of leukemic cells, paving the way to chronic inflammatory diseases and to cancer resurgence, respectively. In both cases, a sexual dimorphism was measured in GSK3β-dependent cellular functions. GSK3β activity is a key marker for inflammatory and cancer diseases allowing adjusted therapy to sex, age and metabolic status of patients.
在成人干细胞中,糖原合酶激酶 3β(GSK3β)处于控制存活、增殖、黏附和分化的信号通路的交汇点。微环境在这些细胞功能的调节中起着关键作用,我们已经证明 GSK3β 的活性强烈依赖于整合素和蛋白酶激活受体(PARs)的参与。整合素 αβ 或 PAR 激活下游,一个分子复合物分别围绕支架蛋白 RACK1 和 β-arrestin-2 组织,包含负责 GSK3β 激活的磷酸酶 PP2A。因此,建立了一种静止的干细胞表型,具有应对凋亡和代谢应激的高能力。已经发现 GSK3β 对造血和肠道干细胞具有保护作用。后者通过 PAR 激活来抵抗去黏附,而前者通过 αβ 结合来抵抗细胞毒性。然而,GSK3β 的长期激活促进了上皮再生缺陷和白血病细胞对化疗的耐药性,分别为慢性炎症性疾病和癌症复发铺平了道路。在这两种情况下,GSK3β 依赖性细胞功能都存在性别二态性。GSK3β 的活性是炎症和癌症疾病的关键标志物,允许根据患者的性别、年龄和代谢状态调整治疗。